MVG Insights
Providing clinical development insight to the biotechnology and pharmaceutical industries
Featured News:
No Results Found
The page you requested could not be found. Try refining your search, or use the navigation above to locate the post.
MVG News:
The Clinical Operations function is a critical component in all studies.
At MVG, our highly-skilled clinical operations consultants have a high level of expertise in the areas of Investigator Recruitment, Site Selection, Regulatory Document Collection, Site Training, Clinical Monitoring (Qualifications, Initiation, Interim, and Close-out...
MVG Clinical Research Associates work closely with your team on protocol and indication training, building strong site relationships and ensuring site compliance.
An MVG Consulting Clinical Research Associate can function as a member of the study team and acts as a link between the study team and the sponsor. Clinical Monitoring is a quality control measure put in place to ensure that the integrity of trial data and well-being...
MVG Consulting is experienced to help at any stage of the Clinical Trial Development process.
MVG Consulting’s Clinical Trial Managers provide leadership and operational expertise through collaborative planning, implementation and execution. MVG Consulting can assist with your Clinical Trial Development by helping sponsors before their study starts, during an...
MVG’s clinical trial management services have helped numerous clients during all phases of project development.
We pride ourselves in providing our clients with fully customized, high quality and cost-effective solutions to meet all of their needs. Contact us to learn more about MVG Consulting and how our team can help your organization achieve your objectives.
From clinical monitoring to SOP development, MVG Consulting provides a variety of vital clinical research operations services for your next project.
MVG provides qualified clinical research professionals who seamlessly become a part of your project team, covering all aspects of clinical development and research.
MVG Consulting assembles entire clinical research teams for small to mid-sized companies engaged in clinical development.
Since 1998, MVG Consulting has been providing companies with alternatives to the large Contract Research Organizations. Services include Clinical Operations, Clinical Monitoring, Clinical Project Management, Clinical Quality Assurance, Data Management, Medical Writing...
MVG provides Hematology Consultants for clinical research.
MVG provides clinical research professionals with expertise in your required therapeutic indications, including hematology. These highly qualified consultants seamlessly become a part of your project team. Additionally, we provide virtual companies with an entire...
While your clinical trial development study is underway, MVG Consulting will keep it on track.
We support ongoing studies in a myriad of ways, including: Site Initiation and Monitoring visits Vendor Management and oversight Protocol Amendments Tracking patient enrollment Clinical Trial Material forecasting In process audits of vendors Review of Monitoring...
MVG provides entire project teams of highly qualified clinical research professionals to virtual companies in the biotech and pharma space.
Services provided include Clinical Research Consulting Services, Clinical Trial Development, Project Rescue, Inspection Readiness, CRO Alternative guidance...essentially, MVG can provide a team that covers all aspects of clinical development.
MVG Consulting Services provides clinical research professionals for biotech and pharmaceutical companies’ clinical development programs.
As an alternative to large CROs, MVG provides highly qualified clinical research professionals who seamlessly become a part of your project team.
Through our staff expertise, MVG Consulting offers clients the highest level of professional service and support.
As an alternative to the large CROs, MVG guides our clients through clinical projects, and help bring them to fruition. For over 20 years, we have helped small to mid-sized biopharmaceutical companies maintain control of their development and conduct successful...
Quality Systems in new companies are generally based on the principles of Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP).
Companies with GLP/GMP-based Quality Systems are often challenged by the possibility of clinical trials and how to adapt their systems to a Good Clinical Practice (GCP) environment. MVG Consulting Services can perform an assessment of what is needed to support...